Research Study for Patients With Neurological Diseases Which Evaluates the Patient Experience of the MemorEM Device
Enrolling by invitation · Not applicable
Conditions studied: Alzheimer Disease, Parkinson Disease, Frontotemporal Dementia, Cortico Basal Degeneration, Posterior Cortical Atrophy (PCA), Neurological Diseases or Conditions, Dementia
In brief
Primary Objective: The primary objective of this pilot study is to gain voluntary feedback from patients with neurological diseases and their caregivers regarding their experiences using the MemorEM head device. This information may help in new designs of the MemorEM and suggest ways to increase compliance for future clinical trials and eventual commercialization. Secondary Objective: The secondary objective is to note areas of potential improvement in the progression of the subject's neurological disease and identify the potential for the MemorEM to treat neurological diseases other than Alzheimer's disease. The investigators are also interested in Alzheimer's variants like those with ApoE4 alleles (none of the participants in the 8-person pilot were Apo-E4 positive), known mutations causing early onset Alzheimer's, and Posterior Cortical Atrophy.
Key facts
- Study ID
- NCT07222605
- Run by
- eQ8Health Corporation d/b/a CareONE Concierge
- People needed
- 1000
- Starts
- 2025-12-01
- Expected to finish
- 2029-12-15
- Last updated by the study team
- 2026-02-05
Who can join
Age: 45 and older, up to 100. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patient diagnosed with a neurological disease involving aggregated proteins such as Alzheimer's and its variants, Parkinson's, Frontotemporal dementia, Amyotrophic lateral sclerosis, Tauopathies, and other related neurological diseases.
- Presence of a caregiver(s) responsible for ensuring treatment compliance and potentially with authority to make medical decisions for the patient if the patient is not competent to make those decisions.
- A statement from each patient's physician that indicates the patient has the ability to understand and consent on their own AND they have the willingness to sign CareONE's patient consent.
You may not qualify if…
- Patient has Seizures, Epilepsy, uncontrolled Depression, uncontrolled Bipolar disorder, psychotic disorders, alcoholism or drug addiction
- Presence of metal implants in the head, except for metal dental implants
- Patient has hypertension that is unresponsive to anti-hypertensive medications
- Patient has implanted medication pumps unless cleared by physician
- Patient has significant heart disease, as determined by a physician
Where it is running
- CareONE Concierge — Atlanta, Georgia, United States
Full record on ClinicalTrials.gov
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